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Nature Genetics|September 1, 1995
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36S A Lynch, P M Bond, A J Copp, et al.Nature Genetics|September 1, 1995
Mutational hotspot in the human biotinidase gene causes profound biotinidase deficiencyR J Pomponio, T R Reynolds, H Cole, et al.Nature Genetics|October 1, 1995
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiationN Patil, D R Cox, D Bhat, et al.Nature Genetics|October 1, 1995
A human parthenogenetic chimaeraL Strain, J P Warner, T Johnston, et al.Nature Genetics|October 1, 1995
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsJ P Struewing, D Abeliovich, T Peretz, et al.Nature Genetics|October 1, 1995
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsyO K Steinlein, J C Mulley, P Propping, et al.Nature Genetics|October 1, 1995
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD familiesNature Genetics|July 1, 1994
Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosisY Yang, F A Nunes, K Berencsi, et al.Nature Genetics|April 1, 1997
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancersP A Steck, M A Pershouse, S A Jasser, et al.Pageof 744